ClinVar Miner

List of variants in gene BARD1 reported as likely benign by University of Washington Department of Laboratory Medicine, University of Washington

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Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_000465.4(BARD1):c.1395+653G>A rs548926631 0.46824
NM_000465.4(BARD1):c.364+4464G>C rs144775419 0.02300
NM_000465.4(BARD1):c.158+3299C>T rs142776370 0.01442
NM_000465.4(BARD1):c.1314+1738A>G rs184892512 0.00862
NM_000465.4(BARD1):c.1569-6730T>C rs11689134 0.00650
NM_000465.4(BARD1):c.1569-6684C>T rs148632364 0.00405
NM_000465.4(BARD1):c.1903+3826A>G rs139399687 0.00368
NM_000465.4(BARD1):c.1677+882T>C rs144407674 0.00272
NM_000465.4(BARD1):c.1977A>G (p.Arg659=) rs147215925 0.00230
NM_000465.4(BARD1):c.364+2098T>C rs182757077 0.00214
NM_000465.4(BARD1):c.1903+2056T>C rs754305525 0.00105
NM_000465.4(BARD1):c.216-206G>A rs145063973 0.00061
NM_000465.4(BARD1):c.364+5275G>A rs559892468 0.00051
NM_000465.4(BARD1):c.1315-3468G>A rs191404429 0.00034
NM_000465.4(BARD1):c.1315-3486T>C rs869312495 0.00028
NM_000465.4(BARD1):c.1569-2280T>G rs186851078 0.00020
NM_000465.4(BARD1):c.2002-11C>T rs187240320 0.00010
NM_000465.4(BARD1):c.1568+1670G>C rs745401077 0.00009
NM_000465.4(BARD1):c.1409A>G (p.Asn470Ser) rs587781976 0.00008
NM_000465.4(BARD1):c.2002-65A>G rs869312497 0.00007
NM_000465.4(BARD1):c.364+3435A>G rs869312498 0.00006
NM_000465.4(BARD1):c.1677+2891T>C rs869312504 0.00002
NM_000465.4(BARD1):c.364+4064G>A rs869312494 0.00002
NM_000465.4(BARD1):c.1568+2615T>G rs869312501 0.00001
NM_000465.4(BARD1):c.158+3314A>G rs869312496 0.00001
NM_000465.4(BARD1):c.1903+1696C>G rs751329195 0.00001
NM_000465.4(BARD1):c.1904-699T>C rs869312502 0.00001
NM_000465.4(BARD1):c.364+2639C>T rs869312500 0.00001
NM_000465.4(BARD1):c.364+720C>A rs869312499 0.00001
NM_000465.4(BARD1):c.1569-6332G>T rs869312503
NM_000465.4(BARD1):c.1903+5872A>C rs576760373
NM_000465.4(BARD1):c.364+3900A>G rs869312505

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